Preethy George

Clinical Research Coordinator @Tekton Research

US

Leading the execution and operational oversight of unblinded clinical trials across Phase studies, focusing on unblinded drug handling and randomization processes. Spearheading site coordination, vendor management, and cross-functional collaboration to drive seamless trial execution and regulatory compliance. Oversaw unblinded operations for Phase clinical trials, ensuring 100% protocol adherence and on-time data submissions across all study sites. Led site readiness initiatives that secured inspection preparedness and achieved zero critical findings during sponsor and regulatory audits. Streamlined informed consent processes, enhancing patient understanding and increasing enrollment efficiency by 15%. Resolved eCRF queries collaboratively, achieving 98% query resolution within 48 hours and optimizing data accuracy. Coordinated cross-functional teams to implement site activation strategies, resulting in faster patient enrollment and data capture. Enhanced monitoring and reporting protocols, ensuring seamless adherence to ICH-GCP guidelines and regulatory standards

Lotus Clinical Research Academy , Karnataka – India

Certiicate in Clinical Research and Pharmacovigilance , Clinical Research and Pharmacovigilance

Bangalore University

Bachelor of Pharmacy - BPharm, Pharmacy

Rajiv Gandhi University of Health Sciences

Master of Pharmacy, Pharmacology and Toxicology

Mahatma Gandhi University

Bachelor Of Science , Zoology/Botany/Chemistry